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Blood Products Blood Products Etiology of bleeding: Platelet Count and function need to be assessed. Coagulation factors Glycoproteins that are synthesized in the liver (except V and VIII – extrahepatic sites) II, VII, IX and X are vit K dependent
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Blood Products • Etiology of bleeding: • Platelet • Count and function need to be assessed. • Coagulation factors • Glycoproteins that are synthesized in the liver (except V and VIII – extrahepatic sites) • II, VII, IX and X are vit K dependent • 2 pathways: intrinsic (PTT) and extrinsic (PT) • Fibrinolysis • Primary fibrinolysis assoc w/ certain urinary tract operations, liver, oral cavity, and post-CPB state.
Blood Products • Etiology of bleeding: • Endothelium • Mechanical
Blood Products – Lab Tests • PTT: • PTT detects abnormalities in prekallikrein, Factors XII, XI, IX, VIII, X, V, II • Prolonged PTT – Hemophilia A & B, Factor XI deficiency, heparin therapy, lupus, acquired anti-8 antibodies • PT: • PT detects abnormalities in Factors II, V, VII, X and fibrinogen
Blood Products – Lab Tests • Both PT & PTT prolonged: • Multiple factors • Selective decrease in one or more common pathway factors • Fibrinogen level < 60-80 mg/dl
Blood Products – Lab Tests • Thrombin time tests clot formation from fibrinogen – dec if fibrinogen is low or abnormal • Bleeding time is variable based on many factors. It is not predictive of surgical bleeding. • Measure of qualitative abnormalities in platelet function and deficiencies • ACT assesses adequacy of heparinization • TEG measures the viscoelastic strength of whole blood as a clot is formed.
Blood Products • Type and screen vs Type and crossmatch: • T&S determines ABO and Rh status and the presence of most commonly encountered antibodies – risk of adverse rxn is 1:1000 • T&S takes about 5 mins • T&C determines ABO and Rh status as well as adverse rxn to even low incidence antigens – risk of rxn is 1:10,000 • T&C takes about 45 mins
Blood Products • T&S: • Type O red cells are mixed with pt serum • Antibody screen • T&C • Type O red cells are mixed with pt serum • Antibody screen • Donor red cells are then mixed with the pt’s serum to determine possible incompatibility
Blood Products – Intra Op Coagulopathies • DIC: • Consumptive coagulopathy presenting as excessive bleeding or intravascular thrombosis • Consumes: • Platelets • Fibrinogen • Factors – V and VIII most frequently exhausted • Diagnosis requires evidence of systemic activation of both procoagulant and fibrinolytic systems, consumption of inhibitors and end organ damage
Blood Products – Intra Op Coagulopathies • DIC: • Lab tests: • Inc PT/PTT – PT > 15 secs • Dec firinogen - < 150 mg% (nml = 150-200) • PLT < 150,000 • Inc D Dimer • Inc Fibrin split products • Treatment: • First treat underlying cause • Treat hypovolemia and acidosis • Heparin in thrombotic states If both increased – specificity = 97% & sensitivity = 100%
Blood Products – Intra Op Coagulopathies • Liver Disease: • coagulopathy • Dec factors • Dec clearance of FSPs PLT dysfunction • Inc fibrinolysis • Treatment – replacement of deficient products and admin of DDAVP to enhance PLT fxn
Blood Products – Intra Op Coagulopathies • Dilutional thrombocytopenia • After replacement of one entire blood volume, only 40% of PLTs remain • One unit of PLTs inc count by 10,000 • Hemolytic transfusion reaction • Suspect in presence of hypotension, hemoglobinuria, or DIC • Resp failure, pulm HTN, dec CO have been reported • Diagnosis is confirmed by the presence of free Hgb in spun plasma using the direct Coomb’s test
Blood Products – Intra Op Coagulopathies • Hemolytic transfusion reaction • Incidence – 1:4,000-6,000; fatal rxn = 1:100,000 • Treatment: • Stop the transfusion • Repeat the crossmatch • Send off blood for free Hgb, PT, PTT, Fibrinogen • Maintain UO with fluids and diuretics
Blood Products – Intra Op Coagulopathies • Vit K deficiency • Effects synthesis of factors II, VII, IX, X, and Protein C & S • The most common cause of prolonged PT in ICU pts – antibiotics (gut flora), malnutrition, fat malabsorption • Emergent therapy - FFP
Blood Products – Transfusion Risks • Infectious risks: • HIV – 1:500,000 • Hep C – 1:103,000 • Hep B – 1:63,000 • Clerical risks – 1:12,000 • Allergic and febrile non-hemolytic reactions • Among the most common • 1-4% develop urticaria • Self-limited
Blood Products – Transfusion Risks • Febrile hemolytic reaction • Inc temp, DIC, hypotension, hemoglobinuria • Anaphylactic reaction • Mediated through antibodies to IgA immunoglobulins that are present in all donor plasma • IgA deficient pts require washed PRBCs • Wheezing and hypotension • Transfusion related sepsis • PLT highest risk b/c at room temp – 100% of PLTs > 5 days old have > 100,000 gm of Staph
Blood Products – Transfusion Risks • Transfusion related sepsis • Most common sepsis with PRBCs • 1. Pseudomonas • 2. Serratia • 3. Yersinia • Transfusion related acute lung injury • 0.02% occurrence • Pts present with hypoxemia, bronchospasm, acute respiratory distress, bil pulm infiltrates • Self-limited – usually resolved in 24-48 hrs
Blood Products – Transfusion Risks • Citrate intoxication • hypocalcemia– hypotension, narrow pulse pressure, inc end diastolic pressure and CVP, tetany • Replete calcium • Autologous transfusion • Best way to avoid transfusion risks • Can donate 1 unit/wk for 4 weeks before surgery
Blood Products – Transfusion Risks • Massive blood transfusion • Defined as replacement of one or more blood volume in a 24 hr period. • Complications (PATCH) • Platelets – dec; Potassium – inc • ARDS; Acidosis • Temp dec • Citrate intoxication • Hepatitis
Blood Products • Order of transfusion • Type specific partial crossmatch • Type specific uncrossmatched • Type O, Rh- - can be used in emergency situations • Transfusion
Blood Products • PRBCs • Indications for PRBC transfusion: • Only one – Increase O2 carrying capacity • 12 million PRBC units transfused/yr and 25% of these are inappropriate transfusions • Always indicated for a Hgb <6 . A healthy pt can tolerate an HCT of 20%, but someone with CAD needs an HCT of at least 30% • High incidence of MI found in anemic pts, with CAD, post-op • 10 ml/kg will inc HCT 10%
Blood Products • PRBCs • 75% of transfused RBCs are in the circulation 24 hrs after transfusion • PRBC HCT = 60% • Preservation • CPD-A (citrate, phosphate, dextrose, adenine) – shelf-life = 35 days at 1-6°C • ADSOL (adenine, dextrose, saline, mannitol) – shelf-life = 42 days • Deglycerolized blood – frozen with glycerol for storage, washed before transfusion
Blood Products • PRBCs • Leucocyte-depleted blood • Washed – IgA deficient
Blood Products • FFP • Contains all soluble coagulation factors • Recommended uses: • Urgent reversal of warfarin therapy • Correction of known coagulation factor deficiencies • Correction of microvascular bleeding in the presence on elevated PT, PTT, and after massive transfusion • Do not use for volume • Antithrombin III def
Blood Products • Cryoprecipitate • Indications • Replace factor VIII (Hemo A), factor XIII, fibrinogen, fibronectin, and vWF
Blood Products • Platelets • Repeated PLT transfusions will lead to anti-PLT antibodies • PLT count and activity are effective for about 2 hours in pts with a production defect. Unknown for consumptive pathology. • Indications: • Pre-op for PLT < 50,000 • Remember that prophylactic transfusion is ineffective in the face of thromobcytopenia 2° to PLT destruction ( ITP)
Blood Products • Platelets • Indications: • Pts with microvascular bleeding whose PLT count is < 50,000 • Pts with a normal PLT count who have PLT dysfunction